Canonical Allele Identifier: CA362724512
Gene: GCM2 HGNC NCBI

Linked Data

dbSNP Id: rs2113249004

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10877139C>T , CM000668.2:g.10877139C>T GRCh38
NC_000006.11:g.10877372C>T , CM000668.1:g.10877372C>T GRCh37
NC_000006.10:g.10985358C>T NCBI36
NG_008970.1:g.9727G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.343+1G>A MANE Select ENSP00000368805.4:n.343+1G>A
ENST00000379491.4:c.343+1G>A ENSP00000368805.4:n.343+1G>A
ENST00000480294.1:c.101-14374C>T ENSP00000417929.1:n.101-14374C>T
NM_004752.3:c.343+1G>A NP_004743.1:n.343+1G>A
XM_011514991.1:c.343+1G>A XP_011513293.1:n.343+1G>A
NM_004752.4:c.343+1G>A MANE Select NP_004743.1:n.343+1G>A